Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate WP_011840397.1 RSPH17029_RS02535 O-succinylhomoserine sulfhydrylase
Query= SwissProt::P9WGB5 (406 letters) >NCBI__GCF_000015985.1:WP_011840397.1 Length = 393 Score = 384 bits (987), Expect = e-111 Identities = 196/384 (51%), Positives = 263/384 (68%), Gaps = 5/384 (1%) Query: 24 VRGGMLRSGFEETAEAMYLTSGYVYGSAAVAEKSFAGE-LDHYVYSRYGNPTVSVFEERL 82 V GG RS + E AEA++LT G+VY SA AE F D ++Y+RYGNPT +FEER+ Sbjct: 12 VHGGSRRSQYGEMAEAIFLTQGFVYDSAEQAEARFIETGADEFIYARYGNPTTRMFEERI 71 Query: 83 RLIEGAPAAFATASGMAAVFTSLGALLGAGDRLVAARSLFGSCFVVCSEILPRWGVQTVF 142 +EG AFATASGMAA+ L +++ AGD LVAAR+LFGSC + E+L R+GV+ F Sbjct: 72 AAVEGTEDAFATASGMAAIHGVLTSIVRAGDHLVAARALFGSCIYILEEVLGRFGVEVTF 131 Query: 143 VDGDDLSQWERALSVPTQAVFFETPSNPMQSLVDIAAVTELAHAAGAKVVLDNVFATPLL 202 VDG DL QW A+ T+AVFFE+ SNP + DI A+ E+AHA GA V++DNVFATP+ Sbjct: 132 VDGTDLDQWRAAVRPGTKAVFFESVSNPTLEVADIGAIAEIAHAVGALVIVDNVFATPVF 191 Query: 203 QQGFPLGVDVVVYSGTKHIDGQGRVLGGAILGDREYIDGPVQKLMRHTGPAMSAFNAWVL 262 G DVV+YS TKHIDGQGR LGG + + +I ++ M+HTG +MS FNAW++ Sbjct: 192 STAVRQGADVVIYSATKHIDGQGRALGGVVCASQAFIRKVLEPFMKHTGGSMSPFNAWLM 251 Query: 263 LKGLETLAIRVQHSNASAQRIAEFLNGHPSVRWVRYPYLPSHPQYDLAKRQMSGGGTVVT 322 L G+ TL +R + +A++IA L GHP + V +P L SHPQ+D+AK QM GT++ Sbjct: 252 LNGMATLDLRCRAMADTAEKIARALEGHPQLGRVIHPALESHPQHDMAKAQMERPGTMI- 310 Query: 323 FALDCPEDVAKQRAFEVLDKMRLIDISNNLGDAKSLVTHPATTTHRAMGPEGRAAIGLGD 382 ALD K+ AF LD ++++ ISNNLGDA+S+ THPATTTH+ + +A +G+ Sbjct: 311 -ALDLAG--GKEAAFRFLDALKIVKISNNLGDARSIATHPATTTHQRLSDAQKAHLGITP 367 Query: 383 GVVRISVGLEDTDDLIADIDRALS 406 G+VR+SVGLED DDLIAD+ +AL+ Sbjct: 368 GLVRLSVGLEDADDLIADLKQALA 391 Lambda K H 0.319 0.135 0.395 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 479 Number of extensions: 21 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 406 Length of database: 393 Length adjustment: 31 Effective length of query: 375 Effective length of database: 362 Effective search space: 135750 Effective search space used: 135750 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory